IP Library Granted Patent US 10,093,900
Granted Patent B2
US 10,093,900 · App. 15/964,446 · Granted Oct 9, 2018

Genetically-modified cells comprising a modified human T cell receptor alpha constant region gene

Inventors: Derek Jantz (Durham, NC); James Jefferson Smith (Morrisville, NC); Michael G. Nicholson (Chapel Hill, NC); Daniel T. MacLeod (Durham, NC); Jeyaraj Antony (Chapel Hill, NC); Victor Bartsevich (Durham, NC)
Assignee: Precision BioSciences, Inc.
C12N5/0636C07K14/7051C07K16/2803C12N15/86C07K2319/01C07K2319/02C07K2319/03C12N2510/00
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Quick Facts
Patent No.
US 10,093,900
App. No.
15/964,446
Granted
Oct 9, 2018
Kind
B2
Abstract

Disclosed herein is a genetically-modified cell comprising in its genome a modified human T cell receptor alpha constant region gene, wherein the cell has reduced cell-surface expression of the endogenous T cell receptor. The present disclosure further relates to methods for producing such a genetically-modified cell, and to methods of using such a cell for treating a disease in a subject.

Claims (13)

1. A pharmaceutical composition comprising a genetically-modified human T cell and a pharmaceutically acceptable carrier, wherein said genetically-modified human T cell comprises in its genome a modified human T cell receptor (TCR) alpha constant region gene, wherein said modified human TCR alpha constant region gene comprises from 5′ to 3′:

(a) a 5′ region of a human TCR alpha constant region gene which is endogenous to said T cell;

(b) an exogenous nucleic acid sequence encoding a chimeric antigen receptor; and

(c) a 3′ region of said human TCR alpha constant region gene which is endogenous to said T cell;

wherein said chimeric antigen receptor comprises a ligand-binding domain having specificity for an antigen present on a cancer cell, and wherein said genetically-modified human T cell expresses said chimeric antigen receptor and exhibits reduced cell-surface expression of the endogenous T cell receptor when compared to unmodified control cells.

2. The pharmaceutical composition of claim 1 , wherein said exogenous nucleic acid sequence comprises a promoter sequence that drives expression of said chimeric antigen receptor.

3. The pharmaceutical composition of claim 1 , wherein said chimeric antigen receptor comprises an intracellular cytoplasmic signaling domain.

4. The pharmaceutical composition of claim 1 , wherein said chimeric antigen receptor comprises an intracellular co-stimulatory signaling domain.

5. The pharmaceutical composition of claim 1 , wherein said chimeric antigen receptor comprises a signal peptide.

6. The pharmaceutical composition of claim 1 , wherein said chimeric antigen receptor comprises a hinge domain.

7. The pharmaceutical composition of claim 1 , wherein said chimeric antigen receptor comprises a transmembrane domain.

8. The pharmaceutical composition of claim 1 , wherein said ligand-binding domain of said chimeric antigen receptor is specific for CD19.

9. The pharmaceutical composition of claim 1 , wherein said exogenous nucleic acid sequence is inserted into said TCR alpha constant region gene which is endogenous to said T cell at a position within SEQ ID NO: 3.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 3, 2018
From: JANTZ, DEREK; SMITH, JAMES JEFFERSON; NICHOLSON, MICHAEL G.; MACLEOD, DANIEL T.; ANTONY, JEYARAJ; BARTSEVICH, VICTOR
To: PRECISION BIOSCIENCES, INC.
Reel/Frame 045703/0112 →
Continuity (5)
Continuation 15865089 · Jan 8, 2018
Continuation PCTUS2016055492 · Oct 5, 2016
Provisional Application 62297426 · Feb 19, 2016
Provisional Application 62237394 · Oct 5, 2015
Related Publication 20180258392A1 · Sep 13, 2018
Cited By (1)
US 12,448,613